Publications by authors named "Vanessa Wermenbol"

8Publications

p.Gly743Val Mutation in COL4A1 Is Responsible for Familial Porencephaly and Severe Hypermetropia.

Front Neurol 2020 11;11:827. Epub 2020 Sep 11.

Neurology Department, ULB-Hôpital Erasme, Université Libre de Bruxelles (ULB), Brussels, Belgium.

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http://dx.doi.org/10.3389/fneur.2020.00827DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516025PMC
September 2020

Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation.

Clin Genet 2020 Jul 28. Epub 2020 Jul 28.

Centre de Référence Neuromusculaire, Department of Neurology, Cliniques Universitaires de Bruxelles Hôpital Erasme, Université Libre de Bruxelles (ULB), Brussels, Belgium.

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http://dx.doi.org/10.1111/cge.13809DOI Listing
July 2020

Altered autonomic control in preterm newborns with impaired neurological outcomes.

Clin Auton Res 2015 Aug 8;25(4):233-42. Epub 2015 Aug 8.

Integrative Physiology of Brain Arousal System, CRNL, INSERM-U1028, CNRS UMR5292, University Lyon 1, Lyon, France.

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http://dx.doi.org/10.1007/s10286-015-0298-6DOI Listing
August 2015

A familial heterozygous null mutation of MET in autism spectrum disorder.

Autism Res 2014 Oct 6;7(5):617-22. Epub 2014 Jun 6.

ULB Center of Human Genetics, Hôpital Erasme, Université Libre de Bruxelles (ULB), Brussels, Belgium; Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (IRIBHM), Université Libre de Bruxelles (ULB), Route de Lennik 808, 1070, Brussels, Belgium.

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http://dx.doi.org/10.1002/aur.1396DOI Listing
October 2014

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

Lancet Neurol 2013 Dec 30;12(12):1159-69. Epub 2013 Oct 30.

Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Sciences Centre (MAHSC), Manchester, UK.

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http://dx.doi.org/10.1016/S1474-4422(13)70258-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349523PMC
December 2013

[A technological platform for cerebral palsy - the ICT4Rehab project].

Med Sci (Paris) 2013 May 28;29(5):529-36. Epub 2013 May 28.

Laboratoire d'anatomie, biomécanique et organogenèse, CP 619, faculté de médecine, Université libre de Bruxelles ULB, 808 route de Lennik, 1070 Bruxelles, Belgique.

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http://dx.doi.org/10.1051/medsci/2013295017DOI Listing
May 2013

Decreased spontaneous arousability in preterm newborns with impaired neurological outcome.

J Sleep Res 2012 Oct;21(5):552-60

Paediatric Department, Centre Hospitalo-Universitaire de Besançon, Université de Franche-Comté, Besançon, France.

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http://dx.doi.org/10.1111/j.1365-2869.2012.01004.xDOI Listing
October 2012